Literature DB >> 2408468

An unstable giant satellite associated with chromosomes 21 and 22 in the same individual.

G K Livingston, J E Lockey, K S Witt, S W Rogers.   

Abstract

The short arms of the acrocentric chromosomes are among the most common sites in which to find human chromosomal heteromorphisms. Heteromorphic chromosomes are noted for their variability between individuals and populations; however, they generally are consistent within an individual. Contrary to this general rule, a normal female was found to have a giant satellite on the short arm of a chromosome 22 in most lymphocytes and fibroblasts, but in other cells, it was attached to a chromosome 21. Furthermore, in some cells, it was found on multiple chromosomes, that is, on both 22's or on a 21 and a 22. The familial nature of this heteromorphism was established when it was found in the woman's mother, where it was confined exclusively to chromosome 22. These results suggest an unstable giant satellite associated with both G-group chromosomes of a normal individual. Results are discussed in the light of the patient's occupational exposure to insecticides at a mushroom farm.

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Year:  1985        PMID: 2408468      PMCID: PMC1684594     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  9 in total

1.  Enlarged satellites as a familial chromosome marker.

Authors:  H L COOPER; K HIRSCHHORN
Journal:  Am J Hum Genet       Date:  1962-06       Impact factor: 11.025

2.  Demonstration of color and size polymorphisms in human acrocentric chromosomes by acridine orange reverse banding.

Authors:  R S Verma; H Dosik; H A Lubs
Journal:  J Hered       Date:  1977 Jul-Aug       Impact factor: 2.645

3.  Letter: Brilliantly fluorescing enlarged short arms D or G.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson; B Noel; B Quack; J Mottet
Journal:  Lancet       Date:  1974-05-25       Impact factor: 79.321

Review 4.  Human chromosomal heteromorphisms: nature and clinical significance.

Authors:  R S Verma; H Dosik
Journal:  Int Rev Cytol       Date:  1980

Review 5.  Autosomal polymorphisms.

Authors:  M A Ferguson-Smith
Journal:  Birth Defects Orig Artic Ser       Date:  1974

6.  Differential Giemsa staining of sister chromatids and the study of chromatid exchanges without autoradiography.

Authors:  S Wolff; P Perry
Journal:  Chromosoma       Date:  1974       Impact factor: 4.316

7.  Human chromosomal heteromorphism in American blacks. V. Racial differences in size variation of the short arm of acrocentric chromosomes.

Authors:  R S Verma; H Dosik
Journal:  Experientia       Date:  1981-03-15

8.  Mitotic recombination and segregation of satellites in Bloom's syndrome.

Authors:  E Therman; P G Otto; N T Shahidi
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

9.  Induction of sister-chromatid exchanges in cultured human cells by an organophosphorous insecticide: malathion.

Authors:  A H Nicholas; M Vienne; H van den Berghe
Journal:  Mutat Res       Date:  1979-06       Impact factor: 2.433

  9 in total
  1 in total

1.  Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes.

Authors:  U Tantravahi; G D Stewart; M Van Keuren; G McNeil; S Roy; D Patterson; H Drabkin; M Lalande; D M Kurnit; S A Latt
Journal:  Hum Genet       Date:  1988-07       Impact factor: 4.132

  1 in total

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